What

Q: MM IV-1 IV-2 III-1 III-2 III-3 A) Using all available information, what is the correct inheritance…

A: Genetic inheritance studies reveal the way a particular gene or a genotype is inherited in the…

Q: A family that exhibits Fragile X syndrome is shown in the pedigree. In the pedigree, squares…

A: Introduction: Fragile X syndrome has triplet repeats at the fragile site. It involves learning…

Q: What do loss of function alleles tell us about normal gene function? Why would a researcher be…

A: Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: 1) Since the process has not yet been perfected, at what stage in the life of a Sickle Cell patient…

A: *Sickle Cell Disease is caused by a single  point mutation in the beta-globin gene, which results in…

Q: Leber congenital amaurosis (LCA) is a form  of congenital blindness in humans and is  known to be…

A: Leber congenital amaurosis (LCA) is a form of congenital blindness in humans and is known to be…

Q: What is a heterochronic mutation? How does it affect the phenotypic outcome of an organism? What…

A: Mutation means sudden changes occur in DNA sequences. The mutation occurs randomly. It also occurs…

Q: In a study of a muscle disorder, several affected families exhibited vision problems, muscle…

A: Genes in nuclear content express most of the characters, while some of the characters are associated…

Q: According to the videos and the readings for this unit, what is true of the gut microbiome? The gut…

A: Gut microbiome are the microbiota (range of bacteria, archea and fungi ) that lives inside the gut…

Q: Meta analysis C9orf72 Known Novel • 20 15 10 SARM1UNC13A МОВР GPX3-TNIP1 -LOC101927815- SCFD1- 5 CO…

A: ALS (Amyotrophic Lateral Sclerosis) is a group of rare neurological disease. It involves  the motor…

Q: How would you explain gene expression? How is it that a particular genotype is actually expressed as…

A: The central dogma is the flow of information that is carried by a gene that is expressed in the form…

Q: Nucleotide Position                   1       5        10        15 Sequence 1. . . . T C T G G A…

A: Haplotypes are referred to the group of alleles that are inherited from a single parent. The…

Q: Why Recessive CF disease alleles either produce no CFTR or produce nonfunctional or less functional…

A: Cystic fibrosis (CF) is a classical example of recessive disease. It is a disease that is inherited.

Q: 1. What is an allele? 2. What is a point mutation? 3. How are point mutations related to alleles?…

A: Note: I have answered These questions based on my knowledge, we are not supposed to answer questions…

Q: One of the two genes known to be mutated in cases of Hypokalemic periodic paralysis (which is…

A: Hypokalemic periodic paralysis is a condition characterized by intermittent episodes of muscle…

Q: Create a typewritten document providing answers to these questions Questions: 1. How does the…

A: Deoxyribonucleic acid, or DNA, is a long double helix made up of two polymer chains of repetitive…

Q: Go to the NCBI’s website at https://ncbi.nlm.nih.gov On the database dropdown menu, select “Gene”…

A: The RB1 gene (Retinoblastoma 1) is a tumor suppressor gene that is located on chromosome 13. The…

Q: polydactyly is an abnormality characterized by webbing between partially or completely duplicated…

A: Given: Need to explain the  abnormality characterized by webbing between partially or completely…

Q: Which of the following has been directly associated with deficiencies in several genes, especially…

A: Introduction snRNPs, or small nuclear ribonucleoproteins, are RNA-protein complexes that combine…

Q: Mutations within the genes for ARSs, are known to be cause certain human maladies, such as the…

A: ARS is an amino-acyl tRNA synthetase that catalyzes the addition of amino acid to the acceptor stem…

Q: In mice, the A allele causes agouti fur, the AY allele causes yellow fur and is dominant to the A…

A: Mutations are alterations in the DNA sequence of an organism. Small changes, such as adding or…

Q: Bloom Syndrome Bloom syndrome is a rare genetic disorder. It is characterized by a short stature…

A: Bloom syndrome is effected by mutations in the BLM gene. Individuals with Bloom syndrome may evolve…

Q: If the effects of mutations 1 +3 is an eye size intermediate between wild type and mutation 1 alone,…

A: DNA or deoxyribonucleic acid is a polymer of deoxyribonucleotides connected together via…

Q: a. What is(are) the difference(s) between orthologs and paralogs? b. What are the main sources of…

A: Orthologs are homologs from different species that catalyse the same enzyme, while paralogs are…

Q: The majority of GWAS associated variants exist in non-coding regions. This has led to additional…

A: Two non-coding mechanisms that contribute to genetic variation and may be associated with non-coding…

Q: Bloom syndrome is an autosomal recessive disease that exhibitshaploinsufficiency. A recent survey…

A: A disease is a state of unhealthiness of the physical body, mind and social interaction. A disease…

Q: Describe how HpaII and MspI can be used to determine if a given DNA sequence is methylated. Any…

A: HpaII and MspI are two useful enzymes used to detect methylation in a given DNA sequence. These…

Q: Why is it difficult to study whether a trait is due to epigenetic changes or due to something else?…

A: The objective of the question is to understand the challenges in studying the role of epigenetic…

Q: What is the NCBI accession number (including the version) of the RefSeq Match for the first…

A: Acession number :  It is distinguishing feature of a RefSeq record is the distinct accession number…

Q: Forward Genetics Analysis uses a variety of beneficial approaches to identify never before described…

A: The term forward genetics is associated with a method that is utilized for studying the genetics…

Mitochondrial Mutations

A mitochondrion is a cellular organelle that serves as the site for cellular respiration and energy production (ATP or Adenosine Triphosphate). It is a double-membrane-bound organelle and is only present in eukaryotic cells.